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Page 1
Toward Ferroelectric Control of Monolayer MoS2.
Nguyen A, Sharma P, Scott T, Preciado E, Klee V, Sun D, Lu IH, Barroso D, Kim S, Shur VY, Akhmatkhanov AR, Gruverman A, Bartels L, Dowben PA. Nguyen A, et al. Among authors: klee v. Nano Lett. 2015 May 13;15(5):3364-9. doi: 10.1021/acs.nanolett.5b00687. Epub 2015 Apr 30. Nano Lett. 2015. PMID: 25909996
Postgrowth tuning of the bandgap of single-layer molybdenum disulfide films by sulfur/selenium exchange.
Ma Q, Isarraraz M, Wang CS, Preciado E, Klee V, Bobek S, Yamaguchi K, Li E, Odenthal PM, Nguyen A, Barroso D, Sun D, von Son Palacio G, Gomez M, Nguyen A, Le D, Pawin G, Mann J, Heinz TF, Rahman TS, Bartels L. Ma Q, et al. Among authors: klee v. ACS Nano. 2014 May 27;8(5):4672-7. doi: 10.1021/nn5004327. Epub 2014 Apr 22. ACS Nano. 2014. PMID: 24684434
2-dimensional transition metal dichalcogenides with tunable direct band gaps: MoS₂(₁-x) Se₂x monolayers.
Mann J, Ma Q, Odenthal PM, Isarraraz M, Le D, Preciado E, Barroso D, Yamaguchi K, von Son Palacio G, Nguyen A, Tran T, Wurch M, Nguyen A, Klee V, Bobek S, Sun D, Heinz TF, Rahman TS, Kawakami R, Bartels L. Mann J, et al. Among authors: klee v. Adv Mater. 2014 Mar 5;26(9):1399-404. doi: 10.1002/adma.201304389. Epub 2013 Dec 12. Adv Mater. 2014. PMID: 24339159
Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomalies.
Stegmann JD, Kalanithy JC, Dworschak GC, Ishorst N, Mingardo E, Lopes FM, Ho YM, Grote P, Lindenberg TT, Yilmaz Ö, Channab K, Seltzsam S, Shril S, Hildebrandt F, Boschann F, Heinen A, Jolly A, Myers K, McBride K, Bekheirnia MR, Bekheirnia N, Scala M, Morleo M, Nigro V, Torella A; TUDP consortium; Pinelli M, Capra V, Accogli A, Maitz S, Spano A, Olson RJ, Klee EW, Lanpher BC, Jang SS, Chae JH, Steinbauer P, Rieder D, Janecke AR, Vodopiutz J, Vogel I, Blechingberg J, Cohen JL, Riley K, Klee V, Walsh LE, Begemann M, Elbracht M, Eggermann T, Stoppe A, Stuurman K, van Slegtenhorst M, Barakat TS, Mulhern MS, Sands TT, Cytrynbaum C, Weksberg R, Isidori F, Pippucci T, Severi G, Montanari F, Kruer MC, Bakhtiari S, Darvish H, Reutter H, Hagelueken G, Geyer M, Woolf AS, Posey JE, Lupski JR, Odermatt B, Hilger AC. Stegmann JD, et al. Among authors: klee v. NPJ Genom Med. 2024 Mar 1;9(1):18. doi: 10.1038/s41525-024-00398-9. NPJ Genom Med. 2024. PMID: 38429302 Free PMC article.
TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila.
Goodman LD, Cope H, Nil Z, Ravenscroft TA, Charng WL, Lu S, Tien AC, Pfundt R, Koolen DA, Haaxma CA, Veenstra-Knol HE, Wassink-Ruiter JSK, Wevers MR, Jones M, Walsh LE, Klee VH, Theunis M, Legius E, Steel D, Barwick KES, Kurian MA, Mohammad SS, Dale RC, Terhal PA, van Binsbergen E, Kirmse B, Robinette B, Cogné B, Isidor B, Grebe TA, Kulch P, Hainline BE, Sapp K, Morava E, Klee EW, Macke EL, Trapane P, Spencer C, Si Y, Begtrup A, Moulton MJ, Dutta D, Kanca O; Undiagnosed Diseases Network; Wangler MF, Yamamoto S, Bellen HJ, Tan QK. Goodman LD, et al. Among authors: klee vh. Am J Hum Genet. 2021 Sep 2;108(9):1669-1691. doi: 10.1016/j.ajhg.2021.06.019. Epub 2021 Jul 26. Am J Hum Genet. 2021. PMID: 34314705 Free PMC article.
13 results